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The E Protein Is a Multifunctional Membrane Protein of SARS-CoV

The E (envelope) protein is the smallest structural protein in all coronaviruses and is the only viral structural protein in which no variation has been detected. We conducted genome sequencing and phylogenetic analyses of SARS-CoV. Based on genome sequencing, we predicted the E protein is a transme...

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Detalles Bibliográficos
Autores principales: Wu, Qingfa, Zhang, Yilin, Lü, Hong, Wang, Jing, He, Ximiao, Liu, Yong, Ye, Chen, Lin, Wei, Hu, Jianfei, Ji, Jia, Xu, Jing, Ye, Jia, Hu, Yongwu, Chen, Wenjun, Li, Songgang, Wang, Jun, Wang, Jian, Bi, Shengli, Yang, Huanming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5172412/
https://www.ncbi.nlm.nih.gov/pubmed/15626343
http://dx.doi.org/10.1016/S1672-0229(03)01017-9
Descripción
Sumario:The E (envelope) protein is the smallest structural protein in all coronaviruses and is the only viral structural protein in which no variation has been detected. We conducted genome sequencing and phylogenetic analyses of SARS-CoV. Based on genome sequencing, we predicted the E protein is a transmembrane (TM) protein characterized by a TM region with strong hydrophobicity and α-helix conformation. We identified a segment (NH(2)-_L-Cys-A-Y-Cys-Cys-N_-COOH) in the carboxyl-terminal region of the E protein that appears to form three disulfide bonds with another segment of corresponding cysteines in the carboxyl-terminus of the S (spike) protein. These bonds point to a possible structural association between the E and S proteins. Our phylogenetic analyses of the E protein sequences in all published coronaviruses place SARS-CoV in an independent group in Coronaviridae and suggest a non-human animal origin.